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The amino acid contents, proportions, and their digestibility by humans characterize a protein's biological value [ 5].
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Malaria, serious relapsing infection in humans, characterized by periodic attacks of chills and fever, anemia, splenomegaly (enlargement of the spleen), and often fatal complications.
Panic disorder is a common illness in humans, characterized by periods of intense anxiety.
Heterozygous mutations in SOX9 cause campomelic dysplasia, a severe skeletal dysmorphology syndrome in humans characterized by a generalized hypoplasia of endochondral bones.
The EDA gene has been reported responsible for X-linked hypohidrotic ectodermal dysplasia (XLHED) in humans characterized by impaired development of hair, eccrine sweat glands, and teeth.
Candida albicans is an important pathogen of humans characterized by a high versatility.
Mutation of FoxP3 leads to immune dysregulation in mice and humans, characterized by lymphoproliferation and autoimmune lesions.
Schnyder corneal dystrophy (SCD) is an autosomal dominant disorder in humans characterized by abnormal accumulation of cholesterol in the cornea.
Psoriasis is an inflammatory, immune disease in humans characterized by the infiltration of chemokines to the skin tissue [ 42].
This is a disease common in both old mice and humans, characterized by fragile skin, easily broken by mild trauma or abrasion.
Heterozygous mutations in TACI are causally linked to IgA and common variable immune deficiencies (CVIDs) in humans, characterized by antibody deficiencies, B lymphopenia and autoimmune manifestations.
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